SHIME®

The SHIME® model is currently the most representative in vitro technology for the combined simulation of the physiological, chemical and microbiological properties of the gastrointestinal tract. The model enables study of the impact of long-term repeated dosing and of the modulation of the microbiota in function of the gut location. The SHIME® can be seen as a clinical trial in vitro, which can provide the spatiotemporal insight into the mechanism of action of a specific treatment, therefore providing complementary data to in vivo studies.

The SHIME® simulates all the compartments of the GI tract, starting with the stomach followed by the small intestine, the proximal and the distal colon (with an option to include the mouth and a specific ileal compartment with ileal microbial community). To be as close as possible to the in vivo situation, the SHIME® model reproduces multiple physiological and microbial in vivo parameters, including body temperature, intestinal volumes, enzyme concentrations, feeding cycles, pH, microbial diversity across anatomical compartments… Due to its flexibility, interindividual variability as well as various specific population groups (babies, children, elderly, healthy and diseased humans, or adjusted to the research question) and even animal models (cats, dogs and pigs) can easily be studied.

In addition to the physically separated proximal and distal colonic reactors, the SHIME® can be extended with the mucosal ‘compartment’ (M-SHIME®) simulating the microenvironment of the gut wall. This extension allows to study the specific roles of the mucosal and the luminal niches in the microbial community. Because of the differences in physiological conditions, these compartments are colonized by specific and differentiated microbial communities. This makes the SHIME® an excellent model to assess the localization of a treatment effect and its temporal onset following multiple daily doses.

To add to the versatility of the applications, the SHIME® technology can also be used to study the impact of repeated dosing on dysbiotic microbial communities for examples from IBD donors, or to study the infection cycle of pathogens. For example, the specific infection cycle of Clostridium difficile, including disease recurrence after vancomycin treatment, can be simulated in a specific application of the SHIME®, the PathoGutTM.

The data that is generated during a SHIME® experiment sheds light on the interplay between test products and the human gut microbiota (microbial composition and activity). When coupled to off-line cell-based assays, the SHIME® can be used to generate data on the effect of a treatment at the level of the epithelial layer and immune parameters. Also the metabolomic profiles or specific metabolites can be screened by coupling the simulation to the in house MetaKey® platform.


Microbial composition analysis

  • qPCR panels and bespoken strain specific qPCR-detection (e.g. to quantify your LBP or probiotic)
  • 16S rRNA gene profiling
  • Shotgun Sequencing
  • Flow cytometry

Microbial activity analysis

  • SCFA, Lactate, Ammonium and pH

Metabolomics: MetaKey® platform

  • LA-REIMS: General screening
  • HPLC-HRMS: Targeted metabolite determination and specific panels

Host-interactions

  • Bioavailability
  • Barrier integrity and immuno-modulatory properties
  • Tight junction proteins and mucin production
  • Wound healing
  • Adhesion/invasion of pathogens

Project-specific detections and analysis

SHIME<sup>®</sup>
Scientific references Picto

Scientific references